Package 69315-281-09

Brand: fenofibric acid

Generic: fenofibric acid
NDC Package

Package Facts

Identity

Package NDC 69315-281-09
Digits Only 6931528109
Product NDC 69315-281
Description

90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (69315-281-09)

Marketing

Marketing Status
Marketed Since 2019-07-18
Brand fenofibric acid
Generic fenofibric acid
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "17afd47a-c2eb-411b-8b6c-6c1ce709dbbf", "openfda": {"nui": ["N0000175596"], "unii": ["BGF9MN2HU1"], "rxcui": ["828373", "828379"], "spl_set_id": ["daa488be-f580-430c-a72c-80ac31bb3e40"], "pharm_class_epc": ["Peroxisome Proliferator Receptor alpha Agonist [EPC]"], "manufacturer_name": ["Leading Pharma, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (69315-281-09)", "package_ndc": "69315-281-09", "marketing_start_date": "20190718"}], "brand_name": "FENOFIBRIC ACID", "product_id": "69315-281_17afd47a-c2eb-411b-8b6c-6c1ce709dbbf", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Peroxisome Proliferator Receptor alpha Agonist [EPC]"], "product_ndc": "69315-281", "generic_name": "FENOFIBRIC ACID", "labeler_name": "Leading Pharma, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "FENOFIBRIC ACID", "active_ingredients": [{"name": "FENOFIBRIC ACID", "strength": "45 mg/1"}], "application_number": "ANDA211626", "marketing_category": "ANDA", "marketing_start_date": "20190718", "listing_expiration_date": "20261231"}